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Nikolay Zernov

Showing results (1-10 of 4) with videos related to

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BMC Medical Genomics|March 16, 2019
Genotype-phenotype correlations in FSHDNikolay Zernov, Mikhail Skoblov
Reproductive Biology and Endocrinology : RB&E|August 22, 2016
Mutations in gonadotropin-releasing hormone signaling pathway in two nIHH patients with successful pregnancy outcomesNikolay Zernov, Mikhail Skoblov, Ancha Baranova, et al.
Diagnostics (Basel, Switzerland)|December 30, 2025
First Symptomatic Pediatric Case of Hb Rothschild (<i>HBB</i>: c.112T>C, p.Trp38Arg): Low-Oxygen-Affinity Hemoglobin Presenting with Persistent PseudohypoxemiaEkaterina Nuzhnaya, Andrey Marakhonov, Artem Ivanov, et al.
American Journal of Human Genetics|April 10, 2026
Bi-allelic WDHD1 variants cause microcephalic primordial dwarfismDebora Tibbe, Marie Ronja Vogt, Tess Holling, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
BMC Medical Genomics|March 16, 2019
Genotype-phenotype correlations in FSHDNikolay Zernov, Mikhail Skoblov
Reproductive Biology and Endocrinology : RB&E|August 22, 2016
Mutations in gonadotropin-releasing hormone signaling pathway in two nIHH patients with successful pregnancy outcomesNikolay Zernov, Mikhail Skoblov, Ancha Baranova, et al.
Diagnostics (Basel, Switzerland)|December 30, 2025
First Symptomatic Pediatric Case of Hb Rothschild (<i>HBB</i>: c.112T>C, p.Trp38Arg): Low-Oxygen-Affinity Hemoglobin Presenting with Persistent PseudohypoxemiaEkaterina Nuzhnaya, Andrey Marakhonov, Artem Ivanov, et al.
American Journal of Human Genetics|April 10, 2026
Bi-allelic WDHD1 variants cause microcephalic primordial dwarfismDebora Tibbe, Marie Ronja Vogt, Tess Holling, et al.
Pageof 1